Publicat the 23 febrer to Hospital Clínic
Today Thursday 23 February was held at the Hospital Clinic of Barcelona giving ceremony Prize for Best Research Project for Fibromyalgia Foundation announces that FF and Science 2011 in cabbage·operation with the Spanish Society of Rheumatology and sponsored by Grünenthal Foundation. This year the award was for Xavier Torres, Fibromyalgia Unit of the Hospital, in M ª Jesús Herrero, Clinical Psychology Service Unit Fibromyalgia Health Park Mar Barcelona, the project entitled ¿Why do people persist with Fibromyalgia in the activity despite increasing pain? The event was attended by Dr.. Josep Brugada, manager Clinic Hospital Medic l', Ms. Emília Altarriba, president of the Foundation and Affected Affected Fibromyalgia and Chronic Fatigue Syndrome; la Dra. Pilar Peris, member of the board of the Spanish Society of Rheumatology; la Dra. Isabel Sanchez Magro, Grünenthal Foundation director, i Mr.. Josep Davins, Deputy Director General of Health Services, Department of Health, together with Dr.. Rafael Manzanera i la Dra. Josefina Jardí, director and manager of the Catalan Institute of Health and Medical Evaluations (ICAM), respectively.
The projecte premiat
It is currently unknown due to fibromyalgia, although there is evidence to suggest that the symptoms of this disease are related to central sensitization of pain transmission system. One factor that may contribute to this awareness is sustained stimulation due to strenuous activity.
People with fibromyalgia have a pattern of behavior characterized by the alternation of short periods of strenuous activity followed by long periods of inactivity. Changing this behavior pattern can reduce the intensity of pain and other symptoms, but patients are resistant to change this pattern, despite their awareness and the pressure they can exert on the environment, disapproving the conduct.
Know the reasons that hinder people with fibromyalgia modify this pattern of persistent activity despite increasing pain. This study aims to build a reliable and valid instrument for measuring beliefs potentially responsible for maintaining the pattern of persistent activity in fibromyalgia; have a guest these features will reduce the number of sessions of assessment and initiate individualized interventions with greater speed and precise.
Read the news on the Web‘Hospital Clínic
With due respect to people who in good faith have believed that the foundation FF and some professionals “Health” work for the good of the people affected and for a true recognition of this disease, Shame is what this study suggests that there is incredible and associations of patients still attend these events and give them your support.
All this hoax of the FF and such studies are aimed at this disease psychologizing, responsible to do the same to the same patient, culpabilizandola for not being willing to change this course pattern that would cause central sensitization. This is more than serious studies ruled out internationally and is ridiculous here continue to maintain, if not for the interest of these sick leave in the hands of psychology, primary care and, above-especially!- no right to a recognition of organic disease (Neuroimmunological) serious, could-and in some cases should- entitle them to an inability.
Mrs. Maite Vivancos is looking (perhaps unknowingly, because otherwise it would be serious) providing coverage and support of these bad intentions of the FF and its president, Emilia Altarriba (who has their interests in all this dark, based on their contacts in Reus, with people who have been behind the whole framework of the hitherto known as Hospitalari de Catalunya Consortium (some of whose members are under investigation for possible favorable treatment, inconsistencies and alleged influence peddling).
Companions, suffering from this serious condition and organic, do not be fooled with pseudoteorías expired and defending the opposite of how interested.
Regards.
Important document denouncing the biggest heist in the history of Catalunya, perpetrated in the Catalan health.
One of the organizations from which it has helped perpetrate such a scandal is now known as Hospitalari de Catalunya Consortium. In this consortium, is the foundation Personalia, of which Emilia is a member of the board Altarriba. The same Emilia Altarriba who heads a foundation of “affected” FM and CFS in which no affected (What nobody is surprised when a woman chairing a foundation dedicated to a disease that neither she nor her family members have not?). Where there's smoke…
Companions, suffering from FM and CFS, in the perdais this document, with the information given in the videos, since we are cheating and swindling all citizens:
http://dempeusperlasalut.wordpress.com/2012/02/26/el-mayor-robo-de-la-historia-de-catalunya/
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I'ma affected FM / CFS / MCS, Today I read the summary published on the research conducted by the Hospital Clinic- IMAS on Fibromyalgia.
Now the question Why do people with Fibromyalgia activity persist despite increasing pain? has left me anonanada… I have no data on the research questions and clear, not refer to activities:
Continue working life?Taking time to care?Continue to raise a family?have a social life?.
They talk about a pattern of difficult behavior to change by the affected. And I wonder: Do all those affected by Fibromyalgia have the same social status,the same degree of disease, work activity and etc.…
One thing I have to give the reason: The causes are still unknown, and there is a cause and effect in the intensity of pain related to physical activity.
In my case, could say that the last 18 months there has been a change in my pattern of activity, I dropped my physical activity both,social,psychic probably a 70-80% of which had been doing. It took three years to tt Number of anxiolytic and antidepressant. And I have not noticed any improvement with respect to pain,or the endless symptoms in patients with these diseases have. I have a long history of diseases associated, which coincidentally are all related to the endocrine system,neurological and inmunulógico. !! And I am treated with antidepressants!!
How affected, I wish that professionals seem to have much interest in seeking an explanation of my behavior patterns before my illness, spend the money of taxpayers to engage seriously investigate organic causes are diseases that cause and that my view is the only way of coping with success.
Dear Lidia.
It's been days that must have answered the writings left on our Web. I have not done before for reasons that are irrelevant, but now I'm in a position to say what I think about your writing.
Call me naive, or a good faith ... neither one nor the other, what I really am is a people who appreciate what others do for me, Federation, by an association, what can be said street level. All that Mrs accounts. Altarriba, the whole time I know it makes, never shown any interest to me than whatever help she can to make things work, despite his poor health. I do not think all the scientific committee formed by the FF are so "dumb" if everything is true accounts continue to work with it. I know most of them and I can only say they are magnificent, dumps in patients, doing talks on holidays without pay, participating in acts selflessly ... if this is to think of them and not in patients, God to come and see. I always think positive and until I prove otherwise give support to those who devoted many hours of his life to research and visits.
Maite Vivancos
presidenta FF2CAt
Mariví.
In the talks I've been with medical researchers, what is certain is that currently there is no drug that is effective even in our infirmities i CFS FM. What is known is that the patients, stop doing normal activities because the body can not stand, but once something recovered, think back to make a living as before and this is to forget; the moment we can not do and the trabajonormalmente, or leave because we get tired ... and has a lot to see the status of every sick person with his personal life, effective, labor, not everyone can rest when we still do what makes us the house, the children ... but clearly it is time to take care of us and do what we can not really force the machine if you do not want to keep getting worse. You think, poorly medicated, anxiolytics and antedepresivos; does not solve the problem of pain, other drugs are more effective and all agree on one thing, is due to walk every day what you can not force the machine.
Maite Vivancos
Presidenta FF2CAT